tezo-A™ titanium cage family

FDA UDI

Class II (US FDA UDI)

by Ulrich GmbH & Co. KG

Identity

Trade Name: tezo-A™ titanium cage family FDA UDI
Generic Name: Metallic spinal interbody fusion cage FDA UDI
Device Name: tezo-A, height 10 mm, length x width 31 x 25 mm, angle 8° FDA UDI
Model / Reference: CS 3433-10 FDA UDI
Description: tezo-A, height 10 mm, length x width 31 x 25 mm, angle 8° FDA UDI

Identifiers

Catalog Number: CS 3433-10 FDA UDI
Primary DI / UDI-DI: 04052536077670 FDA UDI
510(k) Number: K122957 FDA UDI
FDA Product Code: MAX FDA UDI
GMDN Term: Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Metallic spinal interbody fusion cage

tezo-A™ titanium cage family by Ulrich GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Ulrich GmbH & Co. KG

Sources (1)

FDA UDI 69882331-9270-4a17-bcdd-2ecbad0e2240 36 fields · synced May 30, 2026

tezo-A™ titanium cage family

Identity

Identifiers

Classification

Clinical & Handling

Similar devices

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

Manufacturer

Sources (1)